Chemotherapy and Radiation Therapy With or Without Peripheral Stem Cell Transplantation in Treating Patients With Neuroblastoma

Neuroblastoma Study Phase II Study of Various Therapies in Patients With Neuroblastoma

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Peripheral stem cell transplantation may be able to replace immune cells that were destroyed by chemotherapy or radiation therapy used to kill tumor cells. Combining these therapies may kill more tumor cells.

PURPOSE: Phase II trial to study the effectiveness of combining chemotherapy and radiation therapy with or without peripheral stem cell transplantation in treating patients who have neuroblastoma.

Study Overview

Detailed Description

OBJECTIVES:

  • Determine the frequency of spontaneous remission in pediatric patients with localized neuroblastoma.
  • Determine the course of regression in patients with spontaneous remission.
  • Determine the event-free survival rate of patients with high-risk neuroblastoma treated with maintenance chemotherapy OR consolidation chemotherapy followed by autologous stem cell rescue.
  • Determine if a correlation exists between long-term overall survival and catecholamine response in these high-risk patients.
  • Determine if a correlation exists between cytotoxic and conditioning chemotherapies, in terms of bone marrow toxicity, in these high-risk patients.

OUTLINE: This is a multicenter study. Patients are stratified according to risk (low vs standard vs high).

  • Observation stratum (low risk): Patients undergo surgical biopsy followed by observation for 6-12 months. Patients may also undergo second-look surgery. Patients with tumor regression receive no further therapy. Patients with disease progression or no tumor regression receive standard-risk chemotherapy as in the standard-risk stratum.
  • Standard-risk stratum: Patients undergo surgical biopsy. Patients at least 6 months of age receive 1 course of chemotherapy comprising cisplatin IV and etoposide IV continuously on days 1-4 and vindesine IV over 1 hour on day 1. Patients then receive 1 course of chemotherapy comprising vincristine IV over 1 hour on days 1 and 8, dacarbazine IV over 1 hour on days 1-5, ifosfamide IV continuously on days 1-5, and doxorubicin IV over 4 hours on days 6 and 7.

Patients under 6 months of age receive doxorubicin IV over 30 minutes and vincristine IV on days 1, 3, and 5 and cyclophosphamide IV over 5 minutes on days 1-7. Treatment repeats every 3 weeks for 2 courses in the absence of unacceptable toxicity.

After chemotherapy, patients may undergo second-look surgery followed by 2 additional courses of chemotherapy as above. Patients with complete response or very good partial response receive no further therapy. Patients with partial response, minimal response, no response, or progressive disease undergo local radiotherapy daily 5 days a week for approximately 6 weeks. Patients with no response after radiotherapy may then receive therapy as in the high-risk stratum.

  • High-risk stratum: Patients undergo surgical biopsy. Patients at least 6 months of age receive induction chemotherapy comprising cisplatin, etoposide, and vindesine as in the standard-risk stratum combined with filgrastim (G-CSF) subcutaneously (SC) daily beginning on day 8 and continuing until blood counts recover. Patients also receive alternating courses of vincristine, dacarbazine, ifosfamide, and doxorubicin as in the standard-risk stratum combined with G-CSF SC daily beginning on day 9 and continuing until blood counts recover. Treatment repeats every 3 weeks for up to 6 courses in the absence of unacceptable toxicity.

Patients under 6 months of age receive 2 courses of induction chemotherapy as in the standard-risk stratum followed by 4 courses of alternating chemotherapy as above.

Patients may also undergo second-look surgery.

Patients then receive consolidation chemotherapy comprising melphalan IV over 30 minutes on days -8 to -5, etoposide IV over 4 hours on day -4, and carboplatin IV over 1 hour on days -4 to -2. Patients undergo autologous stem cell transplantation (ASCT) on day 0. Patients also receive G-CSF SC or IV over 2 hours daily beginning on day 0. Patients may then undergo radiotherapy daily 5 days a week for 6 weeks.

Patients who were diagnosed less than 1 year ago and who do not demonstrate MYCN amplication receive maintenance chemotherapy comprising oral cyclophosphamide on days 1-8 (instead of consolidation chemotherapy and ASCT as above). Treatment repeats every 3 weeks for 4 courses.

Beginning 4-6 weeks after transplantation or 4 weeks after initiation of the last course of maintenance chemotherapy, all patients receive consolidation therapy with oral tretinoin 3 times daily on days 1-14. Treatment repeats every 28 days for 6 courses followed by a 3-month rest. Patients then receive 3 additional courses.

Patients are followed at 6 weeks, every 3 months for 5 years, and then every 6 months thereafter.

PROJECTED ACCRUAL: Approximately 130 patients (50 in high-risk stratum, 15 in standard-risk stratum, and 65 in observation stratum) will be accrued for this study within 1 year.

Study Type

Interventional

Phase

  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Aachen, Germany, D-52074
        • Urologische Klinik - Universitaetsklinikum Aachen
      • Augsburg, Germany, DOH-86156
        • Zentralklinikum Augsburg
      • Augsburg, Germany, 86154
        • Kinderkrankenhaus Josefinum
      • Bad Mergentheim, Germany, 97980
        • Caritaskrankenhaus
      • Bayreuth, Germany, 95445
        • Klinikum Bayreuth
      • Berlin, Germany, D-13353
        • Charité - Campus Virchow Klinikum
      • Berlin, Germany, 13122
        • Helios Klinikum Berlin
      • Biefeld, Germany, 33617
        • Krankenanstalten Gilead
      • Bonn, Germany, DOH-53113
        • Kinderklinik der Universitaet-Bonn
      • Braunschweig, Germany, 38118
        • Stadt Klinikum - Howedestrase
      • Bremen, Germany, D-28205
        • Zentralkrankenhaus
      • Chemnitz, Germany, D-09116
        • Klinikum Chemnitz GmbH
      • Coburg, Germany, 96450
        • Klinikum Coburg
      • Cologne, Germany, D-50924
        • Medizinische Universitaetsklinik I
      • Cottbus, Germany, D-03048
        • Carl - Thiem - Klinkum Cottbus
      • Datteln, Germany, 45704
        • Vestische Kinderklinik
      • Detmold, Germany, 32756
        • Klinikum Lippe - Detmold
      • Dortmund, Germany, 44123
        • Stadt. Kliniken
      • Dresden, Germany, D-01307
        • Universitatsklinikum Carl Gustav Carl Carus
      • Dresden, Germany, 01229
        • Stadt. KH Dresden - Neustadt
      • Duesseldorf, Germany, D-40225
        • Universitaetsklinik Duesseldorf
      • Erfurt, Germany, 99012
        • HELIOS Klinikum Erfurt GmbH
      • Erlangen, Germany, D-91054
        • Universitaets - Kinderklinik
      • Essen, Germany, D-45122
        • Universitaetsklinikum Essen
      • Frankfurt, Germany, D-60590
        • Klinikum der J.W. Goethe Universitaet
      • Freiburg, Germany, 79106
        • Universitaetskinderklinik - Universitaetsklinikum Freiburg
      • Gelsenkirchen, Germany, 45892
        • Stadt. Kinderklinik
      • Giessen, Germany, D-35385
        • Kinderklinik
      • Goettingen, Germany, D-37075
        • Universitaetsklinikum Goettingen
      • Greiswald, Germany, 17487
        • Universitats - Kinderklinik
      • Gummersbach, Germany, D-51643
        • Kreiskrankenhaus Gummersbach GmbH
      • Halle, Germany, 06003
        • St. Barbara Krankenhaus
      • Halle, Germany, 06097
        • Martin Luther Universitaet
      • Hamburg, Germany, D-20246
        • Universitaets-Krankenhaus Eppendorf
      • Hamburg, Germany, 22763
        • Altonaer Kinderkrankenhaus
      • Hamm, Germany, DOH-59063
        • Evangelische Krankenhaus Hamm
      • Hannover, Germany, D-30625
        • Medizinische Hochschule Hannover
      • Hannover, Germany, 30173
        • Kinderkrankenhaus auf der Bult
      • Heidelberg, Germany, D-69120
        • Universitaets-Kinderklinik Heidelberg
      • Herdecke, Germany, 58313
        • Gemeinschaftskrankenhaus
      • Homburg, Germany, 66421
        • Universitatsklinik Homburg
      • Homburg, Germany, D-66421
        • Marien Hospital
      • Iserlohn, Germany, D-58644
        • Praxis am Evangelischen Krankenhaus Bethanien
      • Jena, Germany, D-07745
        • Universitaets - Kinderklinik
      • Kaiserslautern, Germany, D-67653
        • Westpfalz-Klinikum GmbH
      • Karlsruhe, Germany, 76131
        • Stadt. Kinderklinik
      • Kassel, Germany, D-34125
        • Klinikum Kassel
      • Kassel, Germany, 34121
        • Kinderkrankenhaus
      • Kiel, Germany, D-24105
        • University Hospital Schleswig-Holstein - Kiel Campus
      • Kiel, Germany, 23116
        • Staedtische Krankenhaus Kiel
      • Koblenz, Germany, 56065
        • Stadt. Krankenhaus Kemperhof
      • Koln - Riehl, Germany, D-50735
        • Staedtisches Kinderkrankenhaus
      • Konstanz, Germany, 78461
        • Klinik Konstanz
      • Krefeld, Germany, D-47805
        • Klinikum Krefeld GmbH
      • Leipzig, Germany, 04317
        • Universitaets - Kinderklinik
      • Leipzig, Germany, D-04317
        • Universitaets Klinik fuer Kinderchirurgie
      • Lubeck, Germany, 23538
        • Universitaets - Kinderklinik - Luebeck
      • Ludwigshafen, Germany, 67065
        • St. Annastift Krankenhaus
      • Magdeburg, Germany, 39112
        • Universitatsklinikum der MA
      • Mainz, Germany, D-55131
        • Johannes Gutenberg University
      • Mannheim, Germany, 68167
        • Stadt. Klinik - Kinderklinik
      • Marburg, Germany, 35033
        • Universitaets - Kinderklinik
      • Minden, Germany, D-32423
        • Klinikum Minden
      • Muenster, Germany, D-48149
        • Klinik und Poliklinik fuer Kinderheilkunde - Universitaetsklinikum Muenster
      • Munich, Germany, D-81545
        • Staedtisches Krankenhaus Muenchen - Harlaching
      • Munich, Germany, 80336
        • Universitaets - Kinderpoliklinik
      • Munich, Germany, 80804
        • Kinderklinik d. TU / Schwabing
      • Munich, Germany, DOH-80337
        • Kinderklinik
      • Neunkirchen, Germany, 66539
        • Kinderklinik Kohlhof
      • Nuernberg, Germany, 90419
        • Cnopfche Kinderklinik
      • Oldenburg, Germany, 26133
        • Klinikum Oldenburg
      • Osnabruck, Germany, D-49082
        • Kindershospital
      • Regensburg, Germany, 93049
        • Krankenhaus D Barmherzigen Brueder
      • Rosenheim, Germany, 83022
        • Staedtische Klinikum-Kinderklinik
      • Rostock, Germany, D-18057
        • Kinderklinik - Universitaetsklinikum Rostock
      • Saarbrucken, Germany, 66119
        • Saarbrucker Winterbergkliniken
      • Schwabisch Hall, Germany, 74523
        • Diakone - Krankenhaus
      • Schwerin, Germany, D-19049
        • Klinikum Schwerin
      • Schwienfurt, Germany, 97422
        • Leopoldina - Krankenhaus
      • Siegen, Germany, 57072
        • Deutsches Rotes Kreuz
      • St. Augustin, Germany, 53757
        • Johanniter-Kinderklinik
      • Stuttgart, Germany, DOH-70176
        • Olgahospital
      • Trier, Germany, D-54290
        • Mutterhaus der Borromäerinnen
      • Tuebingen, Germany, D-72076
        • Universitaetsklinikum Tuebingen
      • Ulm, Germany, D-89075
        • Universitaet Ulm
      • Vechta, Germany, D-49377
        • St. Marien Hospital
      • Wilhelmshaven, Germany, 26389
        • Reinhard - Nieter - Krankenhaus
      • Wuerzburg, Germany, D-97080
        • Universitaets - Kinderklinik Wuerzburg
      • Wuppertal, Germany, D-42283
        • Helios Klinikum Wuppertal
      • Maastricht, Netherlands, 6202 AZ
        • Academisch Ziekenhuis Maastricht
      • Basel, Switzerland, CH-4005
        • University Children's Hospital
      • Locarno, Switzerland, 6600
        • Ospedale "la Carita", Locarno
      • Luzerne 16, Switzerland, CH-6000
        • Kinderspital Luzerne
      • Zurich, Switzerland, CH-8032
        • University Children's Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 20 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

DISEASE CHARACTERISTICS:

  • Histologically confirmed neuroblastoma
  • Observation stratum:

    • MYCN gene not amplified
    • Infants with stage I-IVS disease OR
    • Over 1 year of age and stage I or II resectable disease
  • Standard-risk stratum:

    • MYCN gene not amplified
    • Infants with serious symptoms and stage II-IVS disease OR
    • Over 1 year of age with stage II or III unresectable disease
  • High-risk stratum:

    • Stage IV disease OR
    • Stage I-IVS MYCN gene-amplified disease

PATIENT CHARACTERISTICS:

Age:

  • 20 and under

Performance status:

  • Not specified

Life expectancy:

  • Not specified

Hematopoietic:

  • Not specified

Hepatic:

  • Not specified

Renal:

  • No kidney insufficiency

Cardiovascular:

  • No cardiac insufficiency

Other:

  • Not pregnant
  • Fertile patients must use effective contraception
  • No other serious illness

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Not specified

Chemotherapy:

  • No prior chemotherapy within 6 months after diagnosis

Endocrine therapy:

  • Not specified

Radiotherapy:

  • Not specified

Surgery:

  • Not specified

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Frank Berthold, MD, Children's Hospital Medical Center, Cincinnati

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

May 1, 1997

Study Completion (Actual)

February 1, 2002

Study Registration Dates

First Submitted

June 6, 2001

First Submitted That Met QC Criteria

January 26, 2003

First Posted (Estimate)

January 27, 2003

Study Record Updates

Last Update Posted (Estimate)

August 2, 2013

Last Update Submitted That Met QC Criteria

August 1, 2013

Last Verified

August 1, 2002

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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